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SNP Report
Basic Info
| Name | rs897466 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr15:92471253 - 92471253(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.217452 | ||
| Functional Annotation | downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000268164); non_coding_transcript_exon_variant(ENST00000554440); non_coding_transcript_variant(ENST00000554440); upstream_gene_variant(ENST00000556865, ENST00000624458) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
| Approved Symbol | Approved Name | Location | No. of Studies (Positive/Negative/Trend)  |
|---|---|---|---|
| ST8SIA2 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 | 15q26 | 2(2/0/0) |
| C15orf32 | chromosome 15 open reading frame 32 | 15q26.1 | 1(1/0/0) |
Overlap with SZ from cross-disorder studies (count: 0)
Overlap with MDD from cross-disorder studies (count: 0)